EP1460094A1 - Katalysatorzusammensetzung für die Herstellung von Polyurethanharz und Verfahren zu ihrer Herstellung - Google Patents

Katalysatorzusammensetzung für die Herstellung von Polyurethanharz und Verfahren zu ihrer Herstellung Download PDF

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Publication number
EP1460094A1
EP1460094A1 EP04006391A EP04006391A EP1460094A1 EP 1460094 A1 EP1460094 A1 EP 1460094A1 EP 04006391 A EP04006391 A EP 04006391A EP 04006391 A EP04006391 A EP 04006391A EP 1460094 A1 EP1460094 A1 EP 1460094A1
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Prior art keywords
group
catalyst
polyurethane resin
compound
production
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EP04006391A
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English (en)
French (fr)
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EP1460094B1 (de
Inventor
Hiroyuki Kiso
Hiroyuki Yoshimura
Shinichi Inoue
Kouhei Tomita
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Tosoh Corp
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Tosoh Corp
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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08—Processes
    • C08G18/16—Catalysts
    • C08G18/18—Catalysts containing secondary or tertiary amines or salts thereof
    • C08G18/1808—Catalysts containing secondary or tertiary amines or salts thereof having alkylene polyamine groups
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08—Processes
    • C08G18/09—Processes comprising oligomerisation of isocyanates or isothiocyanates involving reaction of a part of the isocyanate or isothiocyanate groups with each other in the reaction mixture
    • C08G18/095—Processes comprising oligomerisation of isocyanates or isothiocyanates involving reaction of a part of the isocyanate or isothiocyanate groups with each other in the reaction mixture oligomerisation to carbodiimide or uretone-imine groups
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08—Processes
    • C08G18/16—Catalysts
    • C08G18/22—Catalysts containing metal compounds
    • C08G18/222—Catalysts containing metal compounds metal compounds not provided for in groups C08G18/225 - C08G18/26

Definitions

  • the present invention relates to a catalyst composition for production of a polyurethane resin and a method for producing a polyurethane resin employing such a catalyst composition.
  • a catalyst composition for production of a polyurethane resin and a method for producing a polyurethane resin employing such a catalyst composition.
  • an organic polyisocyanate is employed, it is possible to produce a polyurethane resin excellent in the curing speed, weather resistance and coating properties.
  • a polyurethane resin is produced commonly by reacting a polyol with an organic polyisocyanate in the presence of a catalyst and, if necessary, a blowing agent, a surfactant, a crosslinking agent, etc. Its curing reaction proceeds even at room temperature, it is possible to form a resin having a crosslinked structure, and it is excellent in the adhesion to a substrate, flexibility and weather resistance. Thus, it is widely used for various applications to e.g. automobiles, buildings, home electric appliances, heavy duty coatings, plastic coatings, adhesives, etc. Especially when an aliphatic isocyanate is employed, its coating tends to scarcely undergo yellowing by light or heat, and it is used for various finish coating materials which are required to have weather resistance. However, as compared with an aromatic isocyanate represented by TDI or MDI, the reaction speed with a polyol is substantially slow, and a catalyst having a higher activity is being required.
  • a tertiary amine catalyst or a metal catalyst is widely used as a catalyst for production of a polyurethane.
  • an organic tin catalyst is used as its activity is high, and dibutyltin dilaurate (hereinafter sometimes referred to as DBTDL) or stannous octoate is mainly used in many cases (e.g. Tetsuo Yokokawa "Structure and Physical Properties of Polyurethanes, and Developments for Higher Functionality and Applications" published by Gijutsu Joho Kyokai, 1998, p.325).
  • transition metal complex type catalysts have been studied as new catalysts.
  • researches for metal acetylacetonate type catalysts have been active (e.g. JP-A-2003-82052, or R.A.Ligabue, "J. Mol. Catal. A. Chem.”, 2000, vol. 157, p.73).
  • a metal acetylacetonate type catalyst represented by iron acetylacetonate or copper acetylacetonate is low in the catalytic activities, and can hardly accomplish the curing speed at a level where an organic tin catalyst is employed.
  • the catalytic activities can be improved over a case where the metal acetylacetonate is used alone, but a catalyst having still higher activities, is desired.
  • a catalyst has been desired which is capable of accomplishing high speed curing of the coating and improving the physical properties of the coating and which can be substituted for an organic tin catalyst.
  • the present inventors have conducted an extensive study on catalysts for polyurethane reactions to improve the curing speed of the organic polyisocyanate and as a result have found a catalyst which is capable of effectively accelerating the reaction of an alcohol with an organic polyisocyanate and which can be substituted for an organic tin catalyst, by using certain specific metal complex catalyst and organic compound in combination.
  • the present invention has been accomplished.
  • the present invention provides a catalyst composition for production of a polyurethane resin and a method for producing a polyurethane resin, as shown below.
  • the catalyst composition for production of a polyurethane resin according to the present invention comprises a metal complex catalyst represented by the above formula (1) and at least one compound selected from the group consisting of a bicyclic tertiary amine compound represented by the above formula (2), a compound having a cumulative double bond, and a quaternary ammonium salt compound.
  • the metal complex catalyst represented by the above formula (1) is an acetylacetonate salt of a metal selected from the group consisting of Mn, Fe, Co, Ni, Cu, Zn, Zr, Ti, Hf, Al and Th, preferably an acetylacetonate salt of a metal selected from the group consisting of Mn, Fe, Co, Ni, Cu, Zr, Ti, Al and Th.
  • manganese acetylacetonate, iron acetylacetonate, cobalt acetylacetonate, nickel acetylacetonate, zirconium acetylacetonate, titanium acetylacetonate, etc. may, for example, be mentioned.
  • manganese(II) acetylacetonate Mn(acac) 2
  • manganese(III) acetylacetonate Mn(acac) 3
  • iron(II) acetylacetonate Fe(acac) 2
  • iron(III) acetylacetonate Fe(acac) 3
  • cobalt(II) acetylacetonate Co(acac) 2
  • nickel(II) acetylacetonate Ni(acac) 2
  • zirconium(IV) acetylacetonate Zr(acac) 4
  • the bicyclic tertiary amine compound represented by the above formula (2) is not particularly limited.
  • it may be 1,8-diazabicyclo[5,4,0]undecene-7, 1,5-diazabicyclo[4,3,0]nonene-5, 1,8-diazabicyclo[5,3,0]decene-7, or 1,4-diazabicyclo[3,3,0]octane-4.
  • 1,8-diazabicyclo[5,4,0]undecene-7 or 1,5-diazabicyclo[4,3,0]nonene-5 is preferred, since it is excellent in catalytic activities and industrially available.
  • the compound having a cumulative double bond is a compound having a double bond system wherein at least three elements are bonded solely by double bonds.
  • a compound is not particularly limited, but may, for example, be an isocyanate, a ketene, an isothiocyanate, a carbodiimide or cumulene.
  • an isocyanate is preferred, since it is excellent in catalytic activities and industrially available.
  • isocyanate hexamethylene diioscyanate, hydrogenated dicyclohexylmethane diisocyanate, hydrogenated xylylene diisocyanate, isophorone diisocyanate, norbornane diisocyanate, 1,3-bis(isocyanate methyl)cyclohexane, L-lysine diisocyanate, 1,6,11-undecane triisocyanate, toluene diisocyanate, diphenylmethane diisocyanate, naphthylene diisocyanate or xylene diisocyanate is preferred.
  • the quaternary ammonium salt compound may be a compound represented by the above formula (3) and is not particularly limited.
  • the quaternary ammonium constituting the quaternary ammonium salt compound represented by the above formula (3) may, for example, be an aliphatic ammonium compound such as tetramethylammonium, methyltriethylammonium, ethyltrimethylammonium, propyltrimethylammonium, butyltrimethylammonium, pentyltrimethylammonium, hexyltrimethylammonium, heptytrimethylammonium, octyltrimethylammonium, nonyltrimethylammonium, decyltrimethylammonium, undecyltrimethylammonium, dodecyltrimethylammonium, tridecyltrimethylammonium, tetradecyltrimethylammonium, heptadecyltrimethylammonium, hexadecyltri
  • tetramethylammonium methyltriethylammonium, ethyltrimethylammonium, butyltrimethylammonium, hexyltrimethylammonium, octyltrimethylammonium, decyltrimethylammonium, dodecyltrimethylammonium, tetradecyltrimethylammonium, hexadecyltrimethylammonium, octadecyltrimethylammonium, (2-hydroxypropyl)trimethylammonium, hydroxyethyltrimethylammonium, 1-methyl-1-azania-4-azabicyclo[2,2,2]octanium or 1,1-dimethyl-4-methylpiperidinium is preferred, since it is excellent in catalytic activities and industrially readily available.
  • the acid constituting the quaternary ammonium salt compound represented by the above formula (3) is not particularly limited, but is preferably, for example, an organic acid group such as a formic group, an acetic group, an octylic group, an oxalic group, a malonic group, a succinic group, a glutaric group, an adipic group, a benzoic group, a toluic group, an ethylbenzoic group, a methylcarbonic group, a phenol group, an alkylbenzenesulfonic group, a toluenesulfonic group, a benzenesulfonic group or a phosphate group, or an inorganic acid group such as a halogen group, a hydroxyl group, a hydrogen carbonic group or a carbonic group.
  • an organic acid group such as a formic group, an acetic group, an octylic group, an oxalic group, a
  • a formic group, an acetic group, an octylic group, a methyl carbonic group, a halogen group, a hydroxyl group, a hydrogen carbonic group and a carbonic group is preferred, since it is excellent in catalytic activities and industrially available.
  • the blend ratio of the metal complex catalyst (A) represented by the above formula (1) to at least one compound (B) selected from the group consisting of the bicyclic tertiary amine compound represented by the above formula (2), the compound having a cumulative double bond, and the quaternary ammonium salt compound represented by the above formula (3) is not particularly limited, but usually, the blend ratio is adjusted so that the molar ratio of (A)/(B) will be within a range of from 20 to 0.05. If the molar ratio exceeds this range, the synergistic effects of the two catalysts may not sometimes be obtained, and there may be a case where no satisfactory performance can be obtained with respect to the coating physical properties and the catalytic activities.
  • the method for producing a polyurethane resin of the present invention comprises reacting a polyol and an organic polyisocyanate in the presence of the above-mentioned catalyst composition of the present invention as a catalyst.
  • the catalyst composition of the present invention is used for the production of a polyurethane resin, it is used usually in an amount within a range of from 0.001 to 10 parts by weight, preferably from 0.01 to 10 parts by weight, per 100 parts by weight of the polyol to be used. If it is less than 0.001 part by weight, the reaction rate tends to be extremely low, and there may be a case where no satisfactory performance can be obtained with respect to the coating physical properties. On the other hand, if it exceeds 10 parts by weight, no additional effect by the increase of the catalyst will be obtained.
  • the metal complex catalyst represented by the above formula (1) and at least one compound selected from the group consisting of a bicyclic tertiary amine represented by the above formula (2), a compound having a cumulative double bond and a quaternary ammonium salt compound represented by (3), to be used as the catalyst composition may preliminarily be mixed and formulated and the formulated composition may be added at the time of the reaction, or they may simultaneously be added at the time of the reaction. Further, they may be used as dissolved in a solvent at the time of mixing.
  • the solvent is not particularly limited, but it may, for example, be an organic solvent of an alcohol such as ethylene glycol, diethylene glycol, dipropylene glycol, propylene glycol or butanediol, a hydrocarbon such as toluene, xylene or mineral turpen, an ester such as ethyl acetate, butyl acetate, methyl glycol acetate or cellosolve acetate, a ketone such as methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, or an amide such as N,N-dimethylformamide or N,N-dimethylacetamide, or a solvent which can be chelated, such as a ⁇ -diketone such as acetylacetone or its fluorinated substituent, a ketoester such as methyl acetoacetate or ethyl acetoacetate.
  • an alcohol such as ethylene glycol, diethylene
  • a catalyst in addition to the catalyst composition of the present invention comprising the metal complex catalyst represented by the above formula (1) and at least one compound selected from the group consisting of the bicyclic tertiary amine compound represented by the above formula (2), the compound having a cumulative double bond, and the quaternary ammonium salt compound represented by the above formula (3), another organic metal catalyst or tertiary amine catalyst may be used in combination within a range not to depart from the concept of the present invention.
  • Such another organic metal catalyst may be an organic metal heretofore known as a catalyst for producing polyurethane and is not particularly limited. Specifically, it may, for example, be an organic tin catalyst such as stannous diacetate, stannous dioctoate, stannous dioleate, stannous dilaurate, dibutyltin oxide, dibutyltin diacetate, dibutyltin dilaurate, dibutyltin dichloride or dioctyltin dilaurate, or nickel octylate, nickel naphthenate, cobale octylate, cobalt naphthenate, bismuth octylate or bismuth naphthenate.
  • an organic tin catalyst such as stannous diacetate, stannous dioctoate, stannous dioleate, stannous dilaurate, dibutyltin oxide, dibutyltin diacetate, dibuty
  • a preferred compound is an organic tin catalyst, and more preferably it is stannous dioctoate or dibutyltin dilaurate.
  • the amount of the organic tin catalyst to be used can be reduced substantially.
  • tertiary amine catalyst may be a conventional tertiary amine catalyst known as a catalyst for production of polyurethane and is not particularly limited. Specifically, it may, for example, be triethylenediamine, 2-methyltriethylenediamine, N,N,N',N'-tetramethylethylenediamine, N,N,N',N'-tetramethylpropylenediamine, N,N,N',N",N"-pentamethyldiethylenetriamine, N,N,N',N",N"-pentamethyl-(3-aminopropyl)ethylenediamine, N,N,N',N",N"-pentamethyldipropylenetriamine, N,N,N',N'-tetramethylhexamethylenediamine, bis(2-dimethylaminoethyl)ether, dimethylethanolamine, dimethylisopropanolamine, dimethylaminoethoxyethanol, N,N-dimethyl-N'
  • the present invention in a case where another organic metal catalyst or another tertiary amine catalyst is used, it is used usually in an amount of from 0.0001 to 5 parts by weight, preferably from 0.001 to 3 parts by weight, per 100 parts by weight of the polyol.
  • the polyol to be used is not particularly limited.
  • a conventional polyether polyol, a polyester polyol, a polycarbonate type polyol, an acrylic polyol, a polybutadiene type polyol, a polyolefin type polyol, a caprolactam modified polyol, a polyester amide polyol, a polyurethane polyol, an epoxy polyol, an epoxy-modified polyol, an alkyd-modified polyol, caster oil or a fluorinated polyol may, for example, be used.
  • These polyols may be used alone or in proper combination as a mixture.
  • the polyether polyol can be produced, for example, by a method, for example, by Gunter Oertel, "Polyurethane Handbook” (1985), Hanser Publishers (Germany), p.42-53 by using as a starting material a compound having at least two active hydrogen groups, such as a polyhydric alcohol such as ethylene glycol, propylene glycol, butylene glycol, tetramethylene glycol, glycerol, trimethylolpropane, pentaerythritol, sorbitol or sucrose, an aliphatic amine compound such as ethylene diamine, an aromatic amine compound such as toluenediamine or diphenylmethane-4,4-diamine, or an alkanolamine such as ethanolamine or diethanolamine, and subjecting it to an addition reaction with an alkylene oxide represented by ethylene oxide or propylene oxide.
  • a polyhydric alcohol such as ethylene glycol, propylene glycol, butylene glycol,
  • the polyester polyol may, for example, be a condensate of a polyhydric alcohol with a polybasic acid such as maleic anhydride, fumaric acid, itaconic anhydride, itaconic acid, adipic acid or isophthalic acid, or a polyester polyol obtained from a waste at the time of production of nylon, a waste of trimethylolpropane or pentaerythritol, a waste of a phthalic acid type polyester, or treatment of a waste product, as disclosed by Keiji Iwata "Polyurethane Resin Handbook" (first edition in 1987), Nikkan Kogyo Shinbunsha, p.116-117.
  • a polybasic acid such as maleic anhydride, fumaric acid, itaconic anhydride, itaconic acid, adipic acid or isophthalic acid
  • a polyester polyol obtained from a waste at the time of production of nylon, a waste of trimethylolpropan
  • the average molecular weight of the polyol is preferably within a range of from 200 to 10,000. If the average molecular weight is less than 200, the distances between crosslinking points tend to be so short that when formed into a coating, the flexibility tends to be inadequate, and the anticracking property tends to be inadequate. If it exceeds 10,000, the crosslinking density tends to be low, and when formed into a coating, the toughness or hardness tends to be inadequate, whereby no adequate effects of the present invention may be obtained.
  • the organic polyisocyanate to be used may be a conventional one and is not particularly limited.
  • an aromatic isocyanate such as toluene diisocyanate (TDI), diphenylmethane diisocyanate (MDI), naphthylene diisocyanate or xylylene diisocyanate
  • an aliphatic isocyanate such as hexamethylene diisocyanate
  • an alicyclic isocyanate such as dicyclohexyl diisocyanate or isophorone diisocyanate
  • a mixture thereof may be mentioned.
  • an aliphatic isocyanate for the purpose of imparting excellent coating physical properties and weather resistance.
  • aliphatic isocyanate a conventional linear aliphatic, cycloaliphatic or alicyclic isocyanate, may be mentioned.
  • an isocyanate such as hexamethylene diisocyanate (hereinafter sometimes referred to simply as HDI), hydrogenated diphenylmethane diisocyanate (hereinafter sometimes referred to simply as H-MDI), hydrogenated xylylene diisocyanate (hereinafter sometimes referred to simply as H-XDI), isophorone diisocyanate (hereinafter sometimes referred to simply as IPDI), norbornane diisocyanate (hereinafter sometimes referred to simply as NBDI), 1,3-bis(isocyanate methyl)cyclohexane (hereinafter sometimes referred to simply as H6XDI), L-lycine diisocyanate (hereinafter sometimes referred to simply as LDI) or 1,6,11-undecane triisocyanate, or a dimer modified product
  • the blocked isocyanate may, for example, be one having active isocyanate groups blocked with e.g. an alcohol such as ethanol, isopropanol or n-butanol, a phenol such as phenol or p-niotrophenol, a lactam such as ⁇ -caprolactam, an oxime such as acetoxime or methyl ethyl ketoxime, or an active methylene-containing compound such as diethyl malonate, ethyl acetoacetate or acetyl acetone.
  • the isocyanate index is not particularly limited, but it is usually within a range of from 50 to 250, more preferably within a range of from 70 to 150. If it is less than 70, the crosslinking density tends to be low, whereby the resin strength tends to be low, and if it exceeds 150, unreacted isocyanate groups tend to remain, whereby the drying property of the coating tends to deteriorate.
  • additives may be used, as the case requires.
  • Such additives may, for example, be a crosslinking agent or a chain extender, a pigment, a colorant, a flame retardant, an aging preventive agent, an antioxidant, a filler, a thickener, a viscosity-reducing agent, a plasticizer, an anti-sagging agent, a precipitation-preventing agent, a defoaming agent, an UV absorber, a solvent, a thixotropic agent, an adsorbent and other known additives.
  • the types and amounts of such additives may suitably be used within the commonly employed ranges so long as they do not depart from known methods and procedures.
  • the crosslinking agent or chain extender may, for example, be a polyhydric alcohol having a low molecular weight (such as ethylene glycol, 1,4-butanediol, 1,3-butanediol, 1,6-hexanediol, glycerol or the like), a low molecular weight amine polyol (such as diethanolamine, triethanolamine or the like), or a polyamine (such as ethylenediamine, diethylenetriamine, piperazine, N-aminoethylpiperazine, xylylene diamine or methylenebisorthochloroaniline).
  • a polyhydric alcohol having a low molecular weight such as ethylene glycol, 1,4-butanediol, 1,3-butanediol, 1,6-hexanediol, glycerol or the like
  • a low molecular weight amine polyol such as diethanolamine, triethanolamine or the like
  • a solvent may be used to dissolve and dilute a material such as an isocyanate or a polyol.
  • a solvent may be an organic solvent, for example, a hydrocarbon such as toluene, xylene or mineral turpen, an ester such as ethyl acetate, butyl acetate, methylglycol acetate or cellosolve acetate, a ketone such as methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, or an amide such as N,N-dimethylformamide or N,N-dimethylacetamide.
  • a hydrocarbon such as toluene, xylene or mineral turpen
  • an ester such as ethyl acetate, butyl acetate, methylglycol acetate or cellosolve acetate
  • a ketone such as methyl ethyl ketone, methyl isobuty
  • the present invention if moisture is present in the system, a foaming phenomenon may take place, or the catalytic activities tend to be weak during the reaction. Accordingly, it is advisable to remove the moisture.
  • the removal of moisture it is preferred that not only the materials such as the polyol, the prepolymer, etc. are subjected to vacuum dehydration under heating, but also an adsorbent such as molecular sieve or zeolite is added to the system.
  • the catalyst composition of the present invention has a high catalytic activity in the urethane-forming reaction, is capable of improving the production rate of a polyurethane product, can be substituted for an organic tin catalyst and thus is industrially extremely effective.
  • HDI-DMF solution Into a 100 ml Erlenmeyer flask flushed with nitrogen, 1.42 g (10.4 mmol) of hexamethylene diisocyanate (HDI) and 50 ml of N,N-dimethylformamide (DMF) were added to prepare a HDI-DMF solution.
  • the DEG-DMF solution and the HDI-DMF solution were respectively stirred for 30 minutes at 30°C, whereupon the HDI-DMF solution was added to the DEG-DMF solution, and the reaction was initiated with stirring.
  • the reaction rate constant k (l/mol-hr) was obtained on the assumption that the reaction of an isocyanate and an alcohol is primary to the respective concentrations. Further, the rate constant Kc (l 2 /eq ⁇ mol ⁇ hr) per catalyst was obtained by dividing the reaction rate constant k by the catalyst concentration. The results are shown in Table 1.
  • Example 1 The same method as in Example 1 was employed except that as a metal complex catalyst, manganese(III) acetylacetonate (Mn(acac) 3 ) was used instead of manganese(II) acetylacetonate (Mn(acac) 2 ) in Example 1.
  • Example 1 The same method as in Example 1 was employed except that as a metal complex catalyst, nickel(II) acetylacetonate was used instead of manganese(II) acetylacetonate in Example 1.
  • Example 1 The same method as in Example 1 was employed except that as a metal complex catalyst, iron(II) acetylacetonate was used instead of manganese(II) acetylacetonate in Example 1.
  • Example 1 The same method as in Example 1 was employed except that zirconium(IV) acetylacetonate was used instead of manganese(II) acetylacetonate in Example 1.
  • Example 1 The same method as in Example 1 was employed except that as a bicyclic tertiary amine compound, 1,5-diazabicyclo[4,3,0]nonene-5 was used instead of 1,8-diazabicyclo[5,4,0]undecene-7 (DBU) in Example 1.
  • DBU 1,8-diazabicyclo[5,4,0]undecene-7
  • Example 1 The same method as in Example 1 was employed except that manganese(II) acetylacetonate as a metal complex catalyst and 1,8-diazabicyclo[5,4,0]undecene-7 (DBU) as a bicyclic tertiary amine compound, were used in a blend ratio as identified in Table 1.
  • DBU 1,8-diazabicyclo[5,4,0]undecene-7
  • Example 1 The same method as in Example 1 was employed except that as a catalyst, a metal complex catalyst or a bicyclic tertiary amine compound was used in the blend ratio as shown in Table 1.
  • Example 1 to 9 by the combination of the specific metal complex catalyst and the bicyclic tertiary amine compound, remarkable improvement in the catalytic activities was observed over the respective single systems (Comparative Examples 1 to 7), the urethane-forming reaction was synergistically accelerated, and a catalytic activity exceeding DBTDL as a tin catalyst, was obtained.
  • Comparative Example 8 which is an Example wherein a conventional catalyst DBTDL was used, DBTDL contains tributyltin as an impurity and can not safely be used from the viewpoint of the environmental hygiene, although the reaction rate constant is high.
  • the mixed and stirred reaction solution was put into an oven having the temperature adjusted to 50°C, and the viscosity profile was measured by using a vibration type viscometer (Viscomate VM-1A-MH, manufactured by Yamaichi Denki K.K.). The time till the viscosity became 1,000 mPa ⁇ s, was taken as a pot life. Further, a reaction solution prepared in the same manner was molded so that the thickness became 1 cm, and cured at 20°C for three days, whereupon the hardness (shore A) of the resin was measured. The results are shown in Table 2.
  • Example 10 The same method as in Example 10 was employed except that the metal complex catalyst and the bicyclic tertiary amine compound were used in the blend ratio as shown in Table 2. The results are also shown in Table 2. COMPARATIVE EXAMPLES 9 to 16
  • Example 10 The same method as in Example 10 was employed except that the metal complex catalyst or the bicyclic tertiary amine compound was used in the blend ratio as shown in Table 2. The results are also shown in Table 2.
  • HDI-DMF solution Into a 20 ml Shlenk tube preliminarily flushed with argon, 0.54 g (4.00 mmol) of hexamethylene diisocyanate (HDI) was charged, and 10 ml of N,N-dimethylformamide (hereinafter sometimes referred to as DMF) was added thereto to prepare a HDI-DMF solution.
  • DMF N,N-dimethylformamide
  • the HDI-DMF solution, the DEG-DMF solution, and the metal complex isocyanate catalyst were respectively stirred for 30 minutes at 30°C, and then, the HDI-DMF solution and the metal complex isocyanate catalyst was added to the three necked flask containing the DEG-DMF solution by means of cannula, whereupon the reaction was initiated with stirring.
  • DBA di-n-butylamine
  • the reaction rate constant k (l/mol ⁇ hr) was obtained on the assumption that the reaction of an isocyanate and an alcohol is primary to the respective concentrations. Further, the rate constant Kc (l 2 /eq ⁇ mol ⁇ hr) per catalyst was obtained by dividing the reaction rate constant k by the catalyst concentration. The results are shown in Table 3.
  • Example 18 The same method as in Example 18 was employed except that as a metal complex catalyst, iron(III) acetylacetonate was used instead of iron(II) acetylacetonate in Example 18. The results are also shown in Table 3.
  • Example 18 The same method as in Example 18 was employed except that as a metal complex catalyst, manganese(II) acetylacetonate was used instead of iron(II) acetylacetonate in Example 18. The results are also shown in Table 3.
  • Example 18 The same method as in Example 18 was employed except that as a metal complex catalyst, manganese(III) acetylacetonate was used instead of iron(II) acetylacetonate in Example 18. The results are also shown in Table 3.
  • Example 18 The same method as in Example 18 was employed except that as a metal complex catalyst, cobalt(II) acetylacetonate was used instead of iron(II) acetylacetonate in Example 18. The results are also shown in Table 3.
  • Example 18 The same method as in Example 18 was employed except that as a metal complex catalyst, zirconium(IV) acetylacetonate was used instead of iron(II) acetylacetonate in Example 18. The results are also shown in Table 3.
  • Example 18 The same method as in Example 18 was employed except that as a compound having a cumulative double bond, 1,3-bis(isocyanate methyl)cyclohexane (H6XDI) was used instead of isophorone diisocyanate (IPDI) in Example 18. The results are also shown in Table 3.
  • H6XDI 1,3-bis(isocyanate methyl)cyclohexane
  • IPDI isophorone diisocyanate
  • Example 18 The same method as in Example 18 was employed except that as a compound having a cumulative double bond, xylene diisocyanate (XDI) was used instead of isophorone diisocyanate (IPDI) in Example 18. The results are also shown in Table 3.
  • XDI xylene diisocyanate
  • IPDI isophorone diisocyanate
  • Example 18 The same method as in Example 18 was employed except that as a catalyst, a metal complex catalyst or a compound having a cumulative double bond was used in a blend ratio as shown in Table 3.
  • Comparative Example 26 which is an Example wherein a conventional catalyst DBTDL was used, DBTDL contains tributyltin as an impurity and can not safely be used from the viewpoint of the environmental hygiene, although the reaction rate constant is high.
  • the mixed and stirred reaction solution was put into an oven having the temperature adjusted to 50°C, and the viscosity profile was measured by using a vibration type viscometer (Viscomate VM-1A-MH, manufactured by Yamaichi Denki K.K.). The time till the viscosity became 1,000 mPa ⁇ s, was taken as a pot life. Further, a reaction solution prepared in the same manner was molded so that the thickness became 1 cm, and cured at 20°C for three days, whereupon the hardness (shore A) of the resin was measured. The results are shown in Table 4.
  • Example 26 The same method as in Example 26 was employed except that the metal complex catalyst and the compound having the cumulative double bond were used in the blend ratio as shown in Table 4. The results are also shown in Table 4.
  • Example 26 The same method as in Example 26 was employed except that the metal complex catalyst or the compound having the cumulative double bond was used in the blend ratio as shown in Table 4. The results are also shown in Table 4.
  • HDI-DMF solution hexamethylene diisocyanate
  • DMF N,N-dimethylformamide
  • the reaction rate constant k (l/mol ⁇ hr) was obtained on the assumption that the reaction of an isocyanate and an alcohol is primary to the respective concentrations. Further, the rate constant Kc (l 2 /eq ⁇ mol ⁇ hr) per catalyst was obtained by dividing the reaction rate constant k by the catalyst concentration. The results are shown in Table 5.
  • Example 36 The same method as in Example 36 was employed except that as a catalyst, the metal complex catalyst and the quaternary ammonium salt compound were used in the blend ratio as identified in Table 5. The results are also shown in Table 5.
  • Example 36 The same method as in Example 36 was employed except that as a catalyst, the metal complex catalyst or the quaternary ammonium salt compound was used in the blend ratio as identified in Table 6. The results are shown in Table 6.
  • the mixed and stirred reaction solution was put into an oven having the temperature adjusted to 50°C, and the viscosity profile was measured by using a vibration type viscometer (Viscomate VM-1A-MH, manufactured by Yamaichi Denki K.K.). The time till the viscosity became 1,000 mPa ⁇ s, was taken as a pot life. Further, a reaction solution prepared in the same manner was molded so that the thickness became 1 cm, and cured at 20°C for three days, whereupon the hardness (shore A) of the resin was measured. The results are shown in Table 7.
  • Example 54 The same method as in Example 54 was employed except that the metal complex catalyst and the quaternary ammonium salt compound were used in the blend ratio as shown in Table 7. The results are also shown in Table 7. COMPARATIVE EXAMPLES 49 to 60
  • Example 54 The same method as in Example 54 was employed except that the metal complex catalyst or the quaternary ammonium salt compound was used in the blend ratio as shown in Table 8. The results are also shown in Table 8.
  • a catalyst composition for production of a polyurethane resin which comprises a metal complex catalyst represented by the following formula (1): M(acac) n (1) wherein M represents Mn, Fe, Co, Ni, Cu, Zn, Zr, Ti, Hf, Al or Th, acac represents acetylacetonate, and n is an integer of from 1 to 4, and at least one compound selected from the group consisting of a bicyclic tertiary amine compound represented by the following formula (2): wherein n is an integer of from 1 to 3, a compound having a cumulative double bond, and a quaternary ammonium salt compound.
  • a metal complex catalyst represented by the following formula (1): M(acac) n (1) wherein M represents Mn, Fe, Co, Ni, Cu, Zn, Zr, Ti, Hf, Al or Th, acac represents acetylacetonate, and n is an integer of from 1 to 4, and at least one compound selected from the group consisting of a bicyclic

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  • Organic Chemistry (AREA)
  • Polyurethanes Or Polyureas (AREA)
EP04006391A 2003-03-18 2004-03-17 Katalysatorzusammensetzung für die Herstellung von Polyurethanharz und Verfahren zu ihrer Herstellung Expired - Lifetime EP1460094B1 (de)

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US20220010165A1 (en) * 2018-11-08 2022-01-13 Ppg Industries Ohio, Inc. Curable Film-Forming Compositions Demonstrating Decreased Cure Time with Stable Pot Life
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US11377517B2 (en) 2013-04-16 2022-07-05 Basf Se Phosphorous containing flame retardants
WO2022263229A1 (de) 2021-06-14 2022-12-22 Basf Se Polyamine als aldehydfänger
WO2023249800A1 (en) 2022-06-21 2023-12-28 Basf Se Polyurethane products with digital functionality through use of embedded sensor devices
WO2024046793A1 (en) 2022-08-31 2024-03-07 Basf Se Process for thermal treatment of a multicomponent plastic waste material
WO2024104923A1 (en) 2022-11-16 2024-05-23 Basf Se Manganese- and iron-containing catalysts comprising an imine ligand for the synthesis of polyurethanes
WO2024213732A1 (en) 2023-04-13 2024-10-17 Basf Se A process for purifying a pyrolysis oil
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WO2022112157A1 (de) 2020-11-25 2022-06-02 Basf Se Polyurethane mit reduzierter aldehydemission
WO2022263229A1 (de) 2021-06-14 2022-12-22 Basf Se Polyamine als aldehydfänger
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